4.5 Article

A High-Quality Grapevine Downy Mildew Genome Assembly Reveals Rapidly Evolving and Lineage-Specific Putative Host Adaptation Genes

期刊

GENOME BIOLOGY AND EVOLUTION
卷 11, 期 3, 页码 954-969

出版社

OXFORD UNIV PRESS
DOI: 10.1093/gbe/evz048

关键词

long reads; oomycete; PacBio; plant-pathogen interactions; Plasmopara viticola

资金

  1. European Commission [FP7-KBBE-311775]
  2. French National Research Agency [ANR-12-ADAP-0009, ANR-13-ADAP-0003, ANR-10-LABX-45]
  3. France Genomique National infrastructure as part of the Investments for the future program [ANR-10-INBS-09]
  4. GET-PACBIO program [Programme operationnel FEDER-FSE MIDI-PYRENEES ET GARONNE 2014-2020]
  5. Agence Nationale de la Recherche (ANR) [ANR-13-ADAP-0003, ANR-12-ADAP-0009] Funding Source: Agence Nationale de la Recherche (ANR)

向作者/读者索取更多资源

Downy mildews are obligate biotrophic oomycete pathogens that cause devastating plant diseases on economically important crops. Plasmopara viticola is the causal agent of grapevine downy mildew, a major disease in vineyards worldwide. We sequenced the genome of Pl. viticola with PacBio long reads and obtained a new 92.94 Mb assembly with high contiguity (359 scaffolds for a N50 of 706.5 kb) due to a better resolution of repeat regions. This assembly presented a high level of gene completeness, recovering 1,592 genes encoding secreted proteins involved in plant-pathogen interactions. Plasmopara viticola had a two-speed genome architecture, with secreted protein-encoding genes preferentially located in gene-sparse, repeat-rich regions and evolving rapidly, as indicated by pairwise dN/dS values. We also used short reads to assemble the genome of Plasmopara muralis, a closely related species infecting grape ivy (Parthenocissus tricuspidata). The lineage-specific proteins identified by comparative genomics analysis included a large proportion of RxLR cytoplasmic effectors and, more generally, genes with high dN/dS values. We identified 270 candidate genes under positive selection, including several genes encoding transporters and components of the RNA machinery potentially involved in host specialization. Finally, the Pl. viticola genome assembly generated here will allow the development of robust population genomics approaches for investigating the mechanisms involved in adaptation to biotic and abiotic selective pressures in this species.

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